Evidence map›Paper›PMID 40954117›Full record

ArticleBritish journal of haematology2025

A novel PML germline variant as a candidate predisposing genetic aberration in familial acute myeloid leukaemia.

Thierry Soussi, Snehangshu Kundu, Pauline Gerbaud, Tatjana Pandzic, Berivan Baskin, Claes Ladenvall, François Delhommeau, Tobias Sjöblom, Panagiotis Baliakas

Abstract read
In one paragraph

Article in British journal of haematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Thierry SoussiDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.ORCID https://orcid.org/0000-0001-8184-3293
Snehangshu KunduDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.ORCID https://orcid.org/0000-0003-3541-5583
Pauline GerbaudSorbonne Université, INSERM, Centre de Recherche Saint-Antoine, CRSA, AP-HP, SIRIC CURAMUS, UMRS_938 Hematopoietic and Leukemic Development, Paris, France.
Tatjana PandzicDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Berivan BaskinDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Claes LadenvallDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.ORCID https://orcid.org/0000-0002-7501-6598
François DelhommeauSorbonne Université, INSERM, Centre de Recherche Saint-Antoine, CRSA, AP-HP, SIRIC CURAMUS, UMRS_938 Hematopoietic and Leukemic Development, Paris, France.ORCID https://orcid.org/0000-0002-4915-0734
Tobias SjöblomDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.ORCID https://orcid.org/0000-0001-6668-4140
Panagiotis BaliakasDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.ORCID https://orcid.org/0000-0002-5634-7156

Funding

ALF Kansliet Uppsala ALF-1002575ALF Kansliet Uppsala ALF-990591ALF Kansliet Uppsala ALF-991381Cancéropole Île-de-France 2019-1-EMERG-22-INSERM 6-1Hadassah-FranceLions CancerFonden 2022-1050146Lions CancerFonden 2023-1050180Svenska Läkaresällskapet SLS-961271Swedish Cancer Foundation 232 745 PjVleugels stiftelse 2020-01
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

acute myeloid leukaemiagenetic analysismolecular diagnosismolecular genetics

Identifiers

PMID40954117
PMCPMC12436221

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.